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Tebuthiuron information


Tebuthiuron[1][2][3][4][5]
Names
Preferred IUPAC name
N-(5-tert-Butyl-1,3,4-thiadiazol-2-yl)-N,N′-dimethylurea
Other names
Spike; Brulan; Brush Bullet; EL-103; Graslan; Perflan; Herbec; Herbic; Reclaim
Identifiers
CAS Number
  • 34014-18-1 checkY
3D model (JSmol)
  • Interactive image
ChEBI
  • CHEBI:81745
ChEMBL
  • ChEMBL1557493
ChemSpider
  • 5190
ECHA InfoCard 100.047.070 Edit this at Wikidata
EC Number
  • 251-793-7
KEGG
  • C18436
PubChem CID
  • 5383
UNII
  • E5OX6GM11E checkY
UN number 3077
CompTox Dashboard (EPA)
  • DTXSID3024316 Edit this at Wikidata
InChI
  • InChI=1S/C9H16N4OS/c1-9(2,3)6-11-12-8(15-6)13(5)7(14)10-4/h1-5H3,(H,10,14)
    Key: HBPDKDSFLXWOAE-UHFFFAOYSA-N
  • InChI=1/C9H16N4OS/c1-9(2,3)6-11-12-8(15-6)13(5)7(14)10-4/h1-5H3,(H,10,14)
    Key: HBPDKDSFLXWOAE-UHFFFAOYAB
SMILES
  • O=C(N(c1nnc(s1)C(C)(C)C)C)NC
Properties
Chemical formula
C9H16N4OS
Molar mass 228.31 g·mol−1
Appearance Off-white to buff-colored crystalline solid
Density 1.186 g/cm3
Melting point 163.19 °C (325.74 °F; 436.34 K) (mean or weighted MP)
Boiling point 394.23 °C (741.61 °F; 667.38 K) (Adapted Stein & Brown method)[who?]
Solubility in water
2500 mg/L
Hazards
Occupational safety and health (OHS/OSH):
Main hazards
dangerous for the environment
GHS labelling:
Pictograms
GHS07: Exclamation markGHS09: Environmental hazard
Signal word
Warning
Hazard statements
H302, H410
Precautionary statements
P264, P270, P273, P301+P312, P330, P391, P501
Safety data sheet (SDS) ChemAdvisor MSDS
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references

Tebuthiuron is a nonselective broad spectrum herbicide of the urea class. It is used to control weeds, woody and herbaceous plants, and sugar cane.[1] It is absorbed by the roots and transported to the leaves, where it inhibits photosynthesis.[4][6] The ingredient was discovered by Air Products and Chemicals, but was registered by Elanco in the United States in 1974, and later sold to Dow AgroSciences.[7]

  1. ^ a b "Pesticide Information Profile Tebuthiuron". Cornell University. Sep 1993. Retrieved 17 February 2011.
  2. ^ "1-(5-tert-butyl-1,3,4-thiadiazol-2-yl)-1,3-dimethylurea". Royal Society of Chemistry. 2011. Retrieved 17 February 2011.
  3. ^ "Tebuthiuron". NIST. 2008. Retrieved 17 February 2011.
  4. ^ a b "Tebuthiuron Herbicide Fact Sheet" (PDF). Bonneville Power Administration. March 2000. Retrieved 17 February 2011.
  5. ^ "InfoCard". ECHA. Retrieved 17 October 2016.
  6. ^ Stephen Enloe; Scott McElroy (15 February 2011). "The Poisoning of Toomer's Oaks" (PDF). Auburn University. Archived from the original (PDF) on 2011-02-20. Retrieved 17 February 2011.
  7. ^ Durkin, Patrick R. (September 22, 2016). "Tebuthiuron: Human Health and Ecological Risk Assessment FINAL REPORT" (PDF). USDA. Syracuse Environmental Research Associates, Inc. Retrieved 19 June 2024.

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